Professional Documents
Culture Documents
Of
Bachelor of Pharmacy B
y
Under supervision
Faculty of Pharmacy
UNITED INSTITUE OF PHARMACY 1
DR. A.P.J. ABDUL KALAM TECHNICAL UNIVERSITY
2021-22
DECALARATION
DATE 28/01/2022
I am thankful to Prof. (Dr.) Alok Mukherjee and Dr. Anil Kumar Sin
gh who has guided me and told me how it will be beneficial for me in m
y future. I am also thankful to all the faculty members for letting aware a
bout the hospitals and the various theories on it. I wish to thank my pare
nts for their undivided support who inspired and encouraged me to go m
y own way. Without them, I would have been unable to complete my trai
ning. At last I want to thank my friends who appreciated me for helping
me during this training in all possible ways and motivating me.
So, my heartiest thank you to all who guided me helped me with all they
could do for me.
1903150500064
Thanking You.
Index
S.No. Content Page No.
1 Introduction 08
2 Hospital Pharmacy 09-10
3 Prescription Monitoring 11
4 Medication Errors & Adverse Drug Reaction Reporting 12
5 Patient Education & Counseling Including Achieving Concordance 13-14
6 Pharmacokinetics & Therapeutic Drug level Monitoring 15
7 The role of Pharmacy Technicians in Clinical Pharmacy Services 16
8 Infrastructure 17
9 General Ward 17
10 Surgical Ward 18
11 Emergency Ward 18
12 Role and responsibility of Hospital Pharmacist 19-21
INTRODUCTION
HOSPITAL PHARMACY
The practice of pharmacy within the hospital under the supervision of a profession
al pharmacist is known as hospital pharmacy.
Page
The routine presence of medical and nursing staff on the ward allows the pharmacis
t to communicate easily with other member so the healthcare team who value the pr
escription-monitoring service that clinical pharmacists provide. 19, 20 Patients’ not
es are also accessible, to enable the pharmacist both to check important information
that may affect their healthcare and to record details of any clinical pharmacy input
made.
Even when the prescribed and administered treatment is correct and no errors have
occurred, a small proportion of patients can still suffer from ADRs. Clinical pharma
cists have an important role to play in the detection and management of ADRs and,
more recently, directly reporting ADRs to the Committee on Safety of Medicines vi
a the Yellow Card scheme. Their involvement can help to increase the number of A
DR reports made, particularly those involving serious reaction.
In recent years, use of the term ‘compliance’ in the context of medication has been
criticized because it implied that patients must simply follow the doctor’s orders, ra
ther than making property informed decisions about their healthcare. The term ‘con
cordance’ has been proposed as a more appropriate description of the situation.
This change in approach helps optimize the benefits of treatment by helping patient
s and clinicians collaborate in a therapeutic partnership.However, if patients are to
make informed choices, then the need for comprehensive patient education become
s more pressing.
Many surveys have found that patients often know little about the medicines they a
re taking. Several studies examining patient counseling and education have shown
that clinical pharmacists can help to improve patients’ knowledge of their treatmen
t. The contribution made can also improve patient adherence to treatment. Improve
d adherence should lead to improved outcomes and evidence has been collected to
demonstrate this.
How patients take their medicines is a crucial component of whether the desired ou
tcomes will be achieved. Key to this is the health beliefs of individuals and the rela
tionship with their healthcare providers that are necessary in order to ensure this ha
ppens. Society is moving away from a paternalistic approach to healthcare to a mor
e empowered one. Thus, whereas a course of treatment used to be accepted obedie
ntly by patients, treatment is now negotiated and options, risks and benefits are dis
cussed and, where necessary, consent is obtained. Thus there is a greater need for i
nformation and education of patients and/or careers in order for them to be able to
make informed decisions about their treatment. Indeed, the 2010 White Paper emp
hasized the importance of patient involvement, and included the phrase ‘nothing ab
out me, without me’.
A number of medicines in common use have a narrow therapeutic index; that is, th
e difference between the lowest effective dose and a potentially toxic dose can be q
uite small. In many cases it is necessary or desirable to undertake therapeutic drug
level monitoring (TDM) to ensure that patients can be treated safely. TDM service
s include the measurement of drug level in the patient’s blood and the application o
f clinical pharmacokinetics to optimize drug therapy.
This is a wide range of medicines that fall into this category, but TDM services typ
ically include amino glycoside antibiotics, anticonvulsants,
immunosuppressant’s, dioxin, lithium and theophylline. Monitoring drug levels in
patients can also provide an important indicator as to whether they are taking their
medicine. Clinical pharmacy input into TDM services can range from the provisio
n of simple advice to other clinicians on when to take samples and how to interpret
results, to fully fledged services that may include collection and laboratory analysi
s of the blood sample.
In a similar manner to the way in which ward pharmacy services provided by phar
macists evolved into clinical pharmacy, pharmacy technicians’ role are becoming i
ncreasingly clinical in nature and can include a wide range of activities.
• Medication supply
• Checking medication in POD schemes
• Patient counseling and education, including the provision of patient aids whe
re appropriate, as well as medication charts and monitored-dose systems to a
id compliance
• Supporting patient’s self-medication
• Medicines information
• Discharge planning for patients, including communication with primary care
colleagues where appropriate
• Involvement in clinical trials and good clinical practice governance
• Preparation of medicines formularies and guidelines
• Training and education
• Liaison with clinical teams on medicines management and expenditure
• AMS.
The importance of AMS is highlighted in national reports and is enshrined within s
tatute in the Health and Social Care Act 2008.
d) General responsibilities:
c) General responsibilities:
In fact, I spent an excellent 150 hour internship, I learned a lot, Observed, Noted, I
dentified, Discussed… I am sure that this information will be useful to me through
out my professional career.
While allowing me better apprehend and manage diseases, and thus serve my count
ry, I shall also transmit them to my successors.
I am satisfied with the internship, and my objectives are reached at 80%, and I than
k once again all those who have contributed to this success.